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SNP Report
| Name | rs553950 dbSNP Ensembl | ||
|---|---|---|---|
| Location | chr8:31933846 - 31933846(1) | ||
| Variant Alleles | T/G | ||
| Ancestral Allele | G | ||
| Minor Allele | T | ||
| Minor Allele Frequence | 0.198283 | ||
| Functional Annotation | intron_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000518104, ENST00000519301, ENST00000520407, ENST00000523534) | ||
| No. of Studies | 2 (Positive: 2; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
| Overlap with SZ? | YES | ||
| Overlap with MDD? | NO | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
| Reference | Statistical Result | Description | Result Category |
|---|---|---|---|
| Thomson, P. A., 2007 | Individual P-value = 0.0288 for SCZ , Individual P-value = 0.0109 for SCZ and BP | This SNP is nominally significant in all three groups: BP, SCZ and combined. | Positive |
| Walker, R. M.,2010 | X2 test:P-value = 0.028 for Scottish 1, P-value = 0.99 for Scottish 2, P-value = 0.093 for merged Scottish | Significant association was found. | Positive |



